Vertaling van "syndrome hurler " (Engels → Frans) :

TERMINOLOGIE

gargoylism | Hunter's syndrome | Hunter-Hurler syndrome | Hurler's disease | Hurler's polydystrophy | Hurler's syndrome | Johnie McL.'s syndrome | Pfaundler-Hurler syndrome | Sheldon-Ellis syndrome | Thompson's syndrome | dysostosis multiplex | dysostotic idiocy | lipochondrodystrophy | mucopolysaccharidosis
gargoylisme | gargoïlisme | dysostosis multiplex | dysostose de type Pfaundler-Hurler | dystrophie de Hurler-Ellis | lipocondrodystrophie | maladie de Hunter-Hurler | maladie de Hurler | maladie de Pfaundler-Hurler | muccopolysaccharidose | nanisme à type de gargouille | syndrome d'Ellis-Sheldon | polydystrophie de Hurler

dysostosis multiplex | gargoylism | Hurler syndrome | Hurler's disease | Hurler's syndrome | lipochondrodystrophy | mucopolysaccharidosis I | mucopolysaccharidosis type I-H | Pfaundler-Hurler syndrome | MPS I [Abbr.] | MPS I-H [Abbr.]
dysostose multiple | gargoylisme | lipochondrodystrophie | maladie de Hurler | mucopolysaccharidose de type I | syndrome de Hurler | syndrome de Pfaundler-Hurler | MPS I [Abbr.] | MPS I-H [Abbr.]

mucopolysaccharidosis IH [ Hurler's syndrome | Hurler-Pfaundler syndrome ]
mucopolysaccharidose de type 1 [ mucopolysaccharidose 1 | maladie de Hurler ]

Syndrome:Hurler | Hurler-Scheie | Scheie
Syndrome de:Hurler | Hurler-Scheie | Scheie

Hurler-Scheie syndrome | mucopolysaccharidosis type I | mucopolysaccharidosis type I H/S | MPS I-H/S [Abbr.]
mucopolysaccharidose de type I | mucopolysaccharidose de type I H/S | syndrome de Hurler-Scheie | MPS I-H/S [Abbr.]

Sturge-Weber syndrome | Dimitri-disease | Kalischer's syndrome | Krabbe's II syndrome | Parkes Weber's syndrome | Sturge's syndrome | Sturge's disease | Sturge-Kalischer-Weber syndrome | Sturge-Weber disease | Sturge-Weber-Dimitri syndrome | Weber-Dimitri syndrome | angioma capillare et venosum calcificans | angiomatosis meningo-oculofacialis | congenital neuroectodermal dysplasia | cutaneocerebral angioma | encephalotrigeminal angiomatosis | encephalotrigeminal syndrome | neurocutaneous syndrome
syndrome de Sturge-Weber | angiomatose encéphalotrigéminée de Sturge-Weber-Krabbe | angiomatose méningo-oculo-faciale | angiomatose neuro-cutanée | angiomatose neuro-oculo-cutanée | maladie de Sturge-Weber-Krabbe | neuro-ectodermo-dysplasie congénitale | syndrome de Brushfield-Wyatt | syndrome neuro-cutané | syndrome de Parkes-Weber | syndrome de Sturge-Weber-Krabbe | syndrome de Weber-Dimitri

Korsakoff's syndrome | Korsakoff syndrome | Korsakov's syndrome | Korsakow's syndrome | alcohol amnestic disorder | alcoholic dementia | amnesic syndrome | amnestic-confabulatory syndrome | amnestic psychosis | amnestic syndrome | cerebropathia psychica toxaemica | chronic alcoholic delirium | dysmnesic psychosis | dysmnesic syndrome | Korsakoff's disease | Korsakoff's psychosis | Korsakoff psychosis | Korsakov's psychosis | Korsakow's psychosis | Korsakosis | polyneuritic insanity | polyneuritic psychosis | polyneuritic syndrome | psychosis polyneuritica
syndrome de Korsakoff | syndrome de Korsakov | cérébropathie toxémique | démence de Meynert | psychose de Korsakoff | psychose de Korsakov | psychopolynévrite | psycho-polynévrite alcoolique | psychose polynévritique de Korsakoff | psychose-polynévrite | syndrome amnésique | syndrome korsakovien

Avellis's syndrome [ Avellis' syndrome | Avellis' paralysis syndrome | Avellis' hemiplegia | Avelli's paralysis | Avellis-Longhi syndrome | ambiguospinothalamic paralysis | ambiguospinothalamic syndrome | spinothalamic tract-nucleus ambiguous syndrome | superior laryngeal nerve syndrome ]
syndrome d'Avellis

gustatory sweating [ auriculotemporal syndrome | Frey's syndrome | Frey syndrome | Von Frey syndrome | Von Frey's syndrome | Baillarger syndrome | gustatory hyperhidrosis | salivosudoriparous syndrome ]
syndrome de Frey [ syndrome de l'auriculotemporal | syndrome du nerf auriculo-temporal | syndrome du nerf auriculotemporal de Frey ]

Bardet-Biedl syndrome | Biedl's syndrome | Biemond's syndrome | Laurence-Moon-Biedl syndrome | Moon-Bardet-Biedl syndrome
syndrome de Laurence-Biedl | syndrome de Laurence-Moon-Bardet

IN-CONTEXT TRANSLATIONS

Every day, these patients are fighting Pompe's disease, Fabry disease, Hurler's syndrome, or Gaucher disease, to name a few.
Ces patients combattent chaque jour la maladie de Pompe, de Fabry, de Hurler, ou de Gaucher, pour ne nommer que celles-ci.

I am talking about $250,000 a year for replacement enzymes to treat Fabry disease or close to $400,000 a year to treat Hurler's syndrome.
On parle d'un montant d'environ 250 000 $ annuellement pour les enzymes de remplacement dans le traitement de la maladie de Fabry ou encore de près de 400 000 $ par année pour traiter le syndrome de Hurler.